(6-Methoxy-naphthalen-1-ylmethyl)-((E)-3-phenyl-allyl)-amine | 1071127-07-5

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: (6-Methoxy-naphthalen-1-ylmethyl)-((E)-3-phenyl-allyl)-amine
• CAS: 1071127-07-5
• 化学式: C₂₁H₂₁NO
• 分子量: 303.404
• InChiKey: KJMRXKUCRMWRGB-RMKNXTFCSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.65
• 重原子数：
  23.0
• 可旋转键数：
  6.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.14
• 拓扑面积：
  21.26
• 氢给体数：
  1.0
• 氢受体数：
  2.0

反应信息

• 作为反应物：
  描述：

  聚合甲醛 、 (6-Methoxy-naphthalen-1-ylmethyl)-((E)-3-phenyl-allyl)-amine 在 sodium tetrahydroborate 作用下， 生成 (E)-N-methyl-N-(3-phenyl-2-propenyl)-6-methoxy-1-naphthalenemethanamine
  参考文献：
  名称：

  Synthesis and structure-activity relationships of naftifine-related allylamine antimycotics

  摘要：

  Naftifine (1) is the first representative of the new antifungal allylamine derivatives. Its biological activity is strictly bound to specific structural requirements that are unrelated to those of known antifungals. A tertiary allylamine function seems to be a prerequisite for activity against fungi. By systematic variation of the individual structural elements in 1, detailed structure-activity relationships are defined in which the phenyl ring is the structural feature permitting the widest variations. Versatile synthetic routes to allylamine derivatives and comparative biological data are presented.

  DOI：

  10.1021/jm00151a019
• 作为产物：
  描述：

  1-(6-甲氧基-1-萘基)甲胺 在 sodium tetrahydroborate 作用下， 以 甲醇 、 苯 为溶剂， 反应 0.33h， 生成 (6-Methoxy-naphthalen-1-ylmethyl)-((E)-3-phenyl-allyl)-amine
  参考文献：
  名称：

  Synthesis and structure-activity relationships of naftifine-related allylamine antimycotics

  摘要：

  Naftifine (1) is the first representative of the new antifungal allylamine derivatives. Its biological activity is strictly bound to specific structural requirements that are unrelated to those of known antifungals. A tertiary allylamine function seems to be a prerequisite for activity against fungi. By systematic variation of the individual structural elements in 1, detailed structure-activity relationships are defined in which the phenyl ring is the structural feature permitting the widest variations. Versatile synthetic routes to allylamine derivatives and comparative biological data are presented.

  DOI：

  10.1021/jm00151a019